US5183582A - Blowing agent-containing polymeric MDI compositions - Google Patents
Blowing agent-containing polymeric MDI compositions Download PDFInfo
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- US5183582A US5183582A US07/891,063 US89106392A US5183582A US 5183582 A US5183582 A US 5183582A US 89106392 A US89106392 A US 89106392A US 5183582 A US5183582 A US 5183582A
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- United States
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- polymeric mdi
- viscosity
- composition
- hcfc
- weight percent
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 21
- 239000004604 Blowing Agent Substances 0.000 title description 6
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000012948 isocyanate Substances 0.000 claims description 12
- 150000002513 isocyanates Chemical class 0.000 claims description 12
- JIABEENURMZTTI-UHFFFAOYSA-N 1-isocyanato-2-[(2-isocyanatophenyl)methyl]benzene Chemical compound O=C=NC1=CC=CC=C1CC1=CC=CC=C1N=C=O JIABEENURMZTTI-UHFFFAOYSA-N 0.000 claims description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 4
- 150000001718 carbodiimides Chemical class 0.000 claims description 3
- 239000006260 foam Substances 0.000 abstract description 9
- 229920002635 polyurethane Polymers 0.000 abstract description 3
- 239000004814 polyurethane Substances 0.000 abstract description 3
- 238000002360 preparation method Methods 0.000 abstract description 3
- 239000005056 polyisocyanate Substances 0.000 abstract 1
- 229920001228 polyisocyanate Polymers 0.000 abstract 1
- 238000009877 rendering Methods 0.000 abstract 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229920005830 Polyurethane Foam Polymers 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011496 polyurethane foam Substances 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- AFYPFACVUDMOHA-UHFFFAOYSA-N chlorotrifluoromethane Chemical compound FC(F)(F)Cl AFYPFACVUDMOHA-UHFFFAOYSA-N 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000021178 picnic Nutrition 0.000 description 1
- 229920000582 polyisocyanurate Polymers 0.000 description 1
- 239000011495 polyisocyanurate Substances 0.000 description 1
- 229920005903 polyol mixture Polymers 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 102220051014 rs141837529 Human genes 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/143—Halogen containing compounds
- C08J9/144—Halogen containing compounds containing carbon, halogen and hydrogen only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
Definitions
- the present invention pertains to isocyanate compositions containing blowing agents. More particularly, the subject invention pertains to compositions comprising medium viscosity polymeric methylenediphenylenediisocyanates (polymeric MDI) and monochlorodifluoromethane.
- polymeric MDI medium viscosity polymeric methylenediphenylenediisocyanates
- monochlorodifluoromethane monochlorodifluoromethane
- Polymeric MDI is a valuable commodity whose largest commercial use is in the preparation of rigid polyurethane foams, particularly insulating foams for refrigerators, freezers, and roofing and siding laminate boards. At present, the majority of such rigid foams are blown with monochlorotrifluoromethane, refrigerant 11, a CFC which has come under increasing disfavor due to its ozone depletion potential. Monochlorodifluorometnane, an HCFC, has been proposed as a substitute for R-11, due to the fact that its ozone depletion potential is only c.a. 5% of R-11. However, R-22 is a gas at room temperature while R-11 is a liquid, and thus its use is problematic.
- Polyol mixtures containing R-22 develop considerable vapor pressure, for example, which can create problems when drums or tank cars are exposed to high temperatures.
- the atmospheric pressure solubility of HCFC-22 in polyester polyols and polyether polyols, for example, is only about 3 and 5 weight percent respectively.
- Polymeric MDI is prepared by the reaction of aniline with formaldehyde, followed by phosgenation and thermal cleavage into a crude mixture of isocyanates.
- the isocyanates prepared according to this process correspond to the formula: ##STR1##
- the content of higher ring-content analogues (n>O) determines to a great extent the viscosity of the mixture.
- the crude reaction mixture is subjected to partial distillation to remove the higher value two ring components. As a result of the distillation, the viscosity of the pot residue increases.
- the end result is the ability of the manufacturer to offer polymeric MDI with a range of viscosities and functionalities, which can be adjusted, if necessary by the addition of lower viscosity polymeric MDI, two-ring MDI, or higher viscosity polymeric MDI.
- the preparation of such polymeric MDI mixtures is well known to those skilled in the art.
- the solubility of gaseous blowing agent in polymeric MDI would be a function of viscosity, either steadily decreasing with higher 2-ring content (lower viscosity) or steadily increasing.
- solubility of HCFC-22 is much greater, at a given pressure, in medium viscosity polymeric MDI, i.e. MDI having a viscosity of from about 400 cps to about 1200 cps, preferably 600 cps to 1000 cps, than polymeric MDI having lower or higher viscosity.
- medium viscosity polymeric MDI mixtures containing HCFC-22 are suitable for preparing polyurethane foams in processes where the use of otherwise similar mixtures containing lower or higher viscosity polymeric MDI would not be suitable due to equipment limitations or safety considerations, particularly in production where the isocyanate component is stored in drums or tanks incapable of withstanding more than modest pressure.
- the medium viscosity polymeric MDI of the subject invention may further contain a minor portion, not to exceed about 30 percent by weight based on the weight of total isocyanate, preferably less than 20 percent by weight and most preferably less than 10 percent by weight of a modified two-ring MDI or modified polymeric MDI wherein the modified MDI or polymeric MDI contains urethane or carbodiimide linkages.
- modified isocyanates are available commercially as LupranateTM MP-102, a urethane modified two-ring MDI, and LupranateTM MM-103, a carbodiimide modified two-ring MDI.
- Other urethane modified MDI's based on polymeric MDI are also available.
- the polyurethane foams prepared from the medium viscosity polymeric MDI/HCFC-22 mixtures are generally of the rigid type, with predominately closed cells, although open cell foams may be suitable for many applications, for example picnic coolers.
- These foams are prepared, as is well known to those skilled in the polyurethane art, by reacting a polyol component generally comprising polyether or polyester polyols with the isocyanate component, at isocyanate indexes of from 70 to 900, preferably 90 to 400. At indexes close to 100, the foam chemistry is such that the predominate linkages are urethane, while at significantly higher indexes, i.e. 200-900, the linkages are predominately isocyanurate.
- Polyisocyanurate foams have been particularly difficult to prepare with gaseous blowing agents, since the small amount of polyol component renders it highly difficult to include the necessary amount of blowing agent. With the medium viscosity polymeric MDI/HCFC-22 mixtures of the subject invention, such foams are possible using nearly conventional technology.
- the foam quality using medium viscosity polymeric MDI/HCFC-22 mixtures may be improved over that expected with higher or lower viscosity polymeric MDI's, particularly the latter, since upon exit from the mix head, the reaction mass, finding itself now at atmospheric pressure, tends to froth, often leading to large "bubbles" rather than fine cells.
- the vapor pressure of HCFC-22 is lower in medium viscosity polymeric MDI at a given HCFC-22 weight percent concentration, these frothing problems can be minimized.
- the pressure at 21° C. (70° F.) is 27.4 psia
- the weight percent of HCFC-22 at 27.4 psia is approximately 6.5 weight percent, approximately 300 percent higher.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
Mixtures of medium viscosity polymeric MDI and HCFC-22 have unexpectedly low vapor pressure, rendering such mixtures suitable for the preparation of polyurethane and polyisocyanate foams.
Description
This is a division of application Ser. No. 07/858,787 filed Mar. 27, 1992.
The present invention pertains to isocyanate compositions containing blowing agents. More particularly, the subject invention pertains to compositions comprising medium viscosity polymeric methylenediphenylenediisocyanates (polymeric MDI) and monochlorodifluoromethane.
Polymeric MDI is a valuable commodity whose largest commercial use is in the preparation of rigid polyurethane foams, particularly insulating foams for refrigerators, freezers, and roofing and siding laminate boards. At present, the majority of such rigid foams are blown with monochlorotrifluoromethane, refrigerant 11, a CFC which has come under increasing disfavor due to its ozone depletion potential. Monochlorodifluorometnane, an HCFC, has been proposed as a substitute for R-11, due to the fact that its ozone depletion potential is only c.a. 5% of R-11. However, R-22 is a gas at room temperature while R-11 is a liquid, and thus its use is problematic. Polyol mixtures containing R-22 develop considerable vapor pressure, for example, which can create problems when drums or tank cars are exposed to high temperatures. The atmospheric pressure solubility of HCFC-22 in polyester polyols and polyether polyols, for example, is only about 3 and 5 weight percent respectively.
One possible solution to this problem is to incorporate R-22 blowing agent in both the polyol component and isocyanate component of the polyurethane system. Unfortunately, the vapor pressure in the isocyanate component can still present a problem.
It has now been unexpectedly discovered that medium viscosity polymeric MDI will hold more R-22 in solution at a given pressure than polymeric MDI having lower or higher viscosities.
Polymeric MDI is prepared by the reaction of aniline with formaldehyde, followed by phosgenation and thermal cleavage into a crude mixture of isocyanates. By suitable selection of the aniline/formaldehyde ratio and the reaction conditions, the amount of two-ring versus higher ring-content analogues can be adjusted. The isocyanates prepared according to this process correspond to the formula: ##STR1## The content of higher ring-content analogues (n>O) determines to a great extent the viscosity of the mixture. Most frequently, the crude reaction mixture is subjected to partial distillation to remove the higher value two ring components. As a result of the distillation, the viscosity of the pot residue increases. The end result is the ability of the manufacturer to offer polymeric MDI with a range of viscosities and functionalities, which can be adjusted, if necessary by the addition of lower viscosity polymeric MDI, two-ring MDI, or higher viscosity polymeric MDI. The preparation of such polymeric MDI mixtures is well known to those skilled in the art.
As the viscosity of the polymeric MDI is determined essentially by the amount of higher ring "polymeric" species, one would expect that the solubility of gaseous blowing agent in polymeric MDI would be a function of viscosity, either steadily decreasing with higher 2-ring content (lower viscosity) or steadily increasing. However, it has unexpectedly been found that such is not the case, and that the solubility of HCFC-22 is much greater, at a given pressure, in medium viscosity polymeric MDI, i.e. MDI having a viscosity of from about 400 cps to about 1200 cps, preferably 600 cps to 1000 cps, than polymeric MDI having lower or higher viscosity. Thus medium viscosity polymeric MDI mixtures containing HCFC-22 are suitable for preparing polyurethane foams in processes where the use of otherwise similar mixtures containing lower or higher viscosity polymeric MDI would not be suitable due to equipment limitations or safety considerations, particularly in production where the isocyanate component is stored in drums or tanks incapable of withstanding more than modest pressure.
The medium viscosity polymeric MDI of the subject invention may further contain a minor portion, not to exceed about 30 percent by weight based on the weight of total isocyanate, preferably less than 20 percent by weight and most preferably less than 10 percent by weight of a modified two-ring MDI or modified polymeric MDI wherein the modified MDI or polymeric MDI contains urethane or carbodiimide linkages. Such modified isocyanates are available commercially as Lupranate™ MP-102, a urethane modified two-ring MDI, and Lupranate™ MM-103, a carbodiimide modified two-ring MDI. Other urethane modified MDI's based on polymeric MDI are also available.
The polyurethane foams prepared from the medium viscosity polymeric MDI/HCFC-22 mixtures are generally of the rigid type, with predominately closed cells, although open cell foams may be suitable for many applications, for example picnic coolers. These foams are prepared, as is well known to those skilled in the polyurethane art, by reacting a polyol component generally comprising polyether or polyester polyols with the isocyanate component, at isocyanate indexes of from 70 to 900, preferably 90 to 400. At indexes close to 100, the foam chemistry is such that the predominate linkages are urethane, while at significantly higher indexes, i.e. 200-900, the linkages are predominately isocyanurate. Polyisocyanurate foams have been particularly difficult to prepare with gaseous blowing agents, since the small amount of polyol component renders it highly difficult to include the necessary amount of blowing agent. With the medium viscosity polymeric MDI/HCFC-22 mixtures of the subject invention, such foams are possible using nearly conventional technology.
Further, the foam quality using medium viscosity polymeric MDI/HCFC-22 mixtures may be improved over that expected with higher or lower viscosity polymeric MDI's, particularly the latter, since upon exit from the mix head, the reaction mass, finding itself now at atmospheric pressure, tends to froth, often leading to large "bubbles" rather than fine cells. As the vapor pressure of HCFC-22 is lower in medium viscosity polymeric MDI at a given HCFC-22 weight percent concentration, these frothing problems can be minimized.
The invention will now be illustrated by the following examples. In the examples, HCFC-22 was metered into a stainless steel bomb having an internal volume of approximately 1 liter containing several stainless steel balls to allow for thorough mixing, and the amount of HCFC-22 added under pressure determined by weighing the bomb. The bomb, in addition to being equipped with an inlet value for HCFC-22 was also equipped with a connection for a pressure transducer. The bomb was evacuated prior to addition of HCFC-22, and thus the pressures measured are in pounds per square inch absolute (psia). In the first two trials, with medium and high viscosity polymeric MDI, the bomb was maintained at 75° F. after each HCFC-22 addition, and shaken several times over a period of approximately one half hour. The pressure was then measured. In trial 3, with low viscosity polymeric MDI, HCFC-22 was added at 2.3 weight percent, and the pressure after equilibration at several temperatures measured. The results are presented below.
TABLE 1
______________________________________
Weight percent HCFC-22 at Pressure
(psia).sup.1
Isocyanate 15 30 45 60 75 90
______________________________________
Medium Viscosity.sup.2
5.0 6.6 8.0 9.5 11.1 12.7
High Viscosity.sup.3
<2.5 4.0 5.7 7.2 -- --
______________________________________
.sup.1 Values interpolated from a plot of pressure versus weight percent.
.sup.2 Lupranate ™ M70L, a polymeric MDI having a nominal viscosity of
700 cps.
.sup.3 Lupranate ™ M200, a polymeric MDI having a nominal viscosity of
2000.
In trial 3, at 2.3 weight percent HCFC-22 concentration in a low viscosity polymeric MDI having a nominal viscosity of 200 cps (Lupranate™ M20S), the pressures (psia) at various temperatures are given below.
TABLE 2
______________________________________
Temperature (°C.)
Pressure (psia)
______________________________________
21 27.4
42 48.5
60 67.7
______________________________________
Thus, at only 2.3 weight percent HCFC-22, the pressure at 21° C. (70° F.) is 27.4 psia, while with medium viscosity polymeric MDI at 75° F. 5° F. higher the weight percent of HCFC-22 at 27.4 psia is approximately 6.5 weight percent, approximately 300 percent higher.
Claims (5)
1. A composition comprising medium viscosity polymeric MDI methylenediphenylenediisocyanate having a viscosity of from 400 to 1200 centipoise when measured at 25° C., and monochlorodifluoromethane.
2. The composition of claim 1 wherein said medium viscosity polymeric methylenediphenylenediisocyante has a viscosity of from 600 to 1000 centipoise when measured at 25° C.
3. The composition of claim 1 wherein said monochlorodifluoromethane is present in an amount of from 4 weight percent to about 12 weight percent based on the total composition.
4. The composition of claim 2 wherein said monochlorodifluoromethane is present in an amount of from 4 weight percent to about 12 weight percent based on the total composition.
5. The composition of claim 1, further comprising a minor quantity, not to exceed 30 percent by weight of total isocyanate of a modified tow-ring methylenediphenylenediisocyanode or modified polymeric methlenediphenylenediisocyanode wherein said modified methylenediphenylenediisocyanate or polymeric methylenediphenylenediisocyanate contains urethane or carbodiimide linkages.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/891,063 US5183582A (en) | 1992-03-27 | 1992-06-01 | Blowing agent-containing polymeric MDI compositions |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/858,787 US5182311A (en) | 1992-03-27 | 1992-03-27 | Blowing agent-containing polymeric MDI compositions |
| US07/891,063 US5183582A (en) | 1992-03-27 | 1992-06-01 | Blowing agent-containing polymeric MDI compositions |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/858,787 Division US5182311A (en) | 1992-03-27 | 1992-03-27 | Blowing agent-containing polymeric MDI compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5183582A true US5183582A (en) | 1993-02-02 |
Family
ID=27127482
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/891,063 Expired - Fee Related US5183582A (en) | 1992-03-27 | 1992-06-01 | Blowing agent-containing polymeric MDI compositions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US5183582A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2025046142A1 (en) * | 2023-09-03 | 2025-03-06 | Kingspan Holdings (Irl) Limited | Polyurethane foams and methods of manufacture thereof |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4205136A (en) * | 1978-02-21 | 1980-05-27 | Bridgestone Tire Company Limited | Process for producing a rigid polyurethane foam having excellent flame retardance and low-smoke development |
| US4218543A (en) * | 1976-05-21 | 1980-08-19 | Bayer Aktiengesellschaft | Rim process for the production of elastic moldings |
| US4452924A (en) * | 1983-05-05 | 1984-06-05 | Mobay Chemical Corporation | Flexible polyurethane foams having improved load bearing characteristics |
| US4546122A (en) * | 1984-08-06 | 1985-10-08 | Mobay Chemical Corporation | Flexible polyurethane foams |
| US4713399A (en) * | 1985-12-30 | 1987-12-15 | The Dow Chemical Company | Flexible polyurethane foams prepared from poly(alkylene carbonate) polyols |
| US4927863A (en) * | 1988-02-22 | 1990-05-22 | E. I. Du Pont De Nemours And Company | Process for producing closed-cell polyurethane foam compositions expanded with mixtures of blowing agents |
| US4980388A (en) * | 1988-10-17 | 1990-12-25 | The Dow Chemical Company | Use of carbon dioxide adducts as blowing agents in cellular and microcellular polyureas |
-
1992
- 1992-06-01 US US07/891,063 patent/US5183582A/en not_active Expired - Fee Related
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4218543A (en) * | 1976-05-21 | 1980-08-19 | Bayer Aktiengesellschaft | Rim process for the production of elastic moldings |
| US4205136A (en) * | 1978-02-21 | 1980-05-27 | Bridgestone Tire Company Limited | Process for producing a rigid polyurethane foam having excellent flame retardance and low-smoke development |
| US4452924A (en) * | 1983-05-05 | 1984-06-05 | Mobay Chemical Corporation | Flexible polyurethane foams having improved load bearing characteristics |
| US4546122A (en) * | 1984-08-06 | 1985-10-08 | Mobay Chemical Corporation | Flexible polyurethane foams |
| US4713399A (en) * | 1985-12-30 | 1987-12-15 | The Dow Chemical Company | Flexible polyurethane foams prepared from poly(alkylene carbonate) polyols |
| US4927863A (en) * | 1988-02-22 | 1990-05-22 | E. I. Du Pont De Nemours And Company | Process for producing closed-cell polyurethane foam compositions expanded with mixtures of blowing agents |
| US4980388A (en) * | 1988-10-17 | 1990-12-25 | The Dow Chemical Company | Use of carbon dioxide adducts as blowing agents in cellular and microcellular polyureas |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2025046142A1 (en) * | 2023-09-03 | 2025-03-06 | Kingspan Holdings (Irl) Limited | Polyurethane foams and methods of manufacture thereof |
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